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Newborn Screening Plus (Including CF)
An integrated screening program including cystic fibrosis, endocrine, and metabolic disorder detection, giving your baby the best possible healthy start through early and accurate diagnosis.

A newborn screening program involves analyzing a blood sample taken from the baby's heel to detect a range of serious congenital disorders. This typically includes screening for congenital hypothyroidism, cystic fibrosis (CF), metabolic disorders of amino acids and organic acids, and fatty acid oxidation, as well as other conditions as determined by the national program.
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